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Searched for days. Results 861 to 870 of 1849 total matches.

Lazertinib (Lazcluze) for Non-Small Cell Lung Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Oct 28, 2024  (Issue 1714)
and the risk of adverse effects. ▶ Dosage: 240 mg once daily. ▶ Cost: A 30-day supply costs $18,198 ...
Lazertinib (Lazcluze – Janssen Biotech), an oral kinase inhibitor, has been approved by the FDA for use in combination with the EGFR-MET bispecific antibody amivantamab (Rybrevant) for first-line treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) in adults with epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R substitution mutations. This is the first approval for Lazcluze; amivantamab was previously approved for use alone and in combination with carboplatin and pemetrexed for treatment of NSCLC with EGFR exon 20 insertion...
Med Lett Drugs Ther. 2024 Oct 28;66(1714):e176-7   doi:10.58347/tml.2024.1714g |  Show IntroductionHide Introduction

Eszopiclone (Lunesta), a New Hypnotic

   
The Medical Letter on Drugs and Therapeutics • Feb 28, 2005  (Issue 1203)
. They can cause residual adverse effects the next day, dependence, rebound insomnia, and withdrawal ...
Eszopiclone (Lunesta - Sepracor), a benzodiazepine-like drug, has been approved by the FDA for oral treatment of insomnia. It is the S-isomer of zopiclone (Imovane, and others in Canada), which has been available in other countries for almost 20 years. Unlike similar drugs such as zolpidem (Ambien) or zaleplon (Sonata), Lunesta is not being restricted in its labeling to short-term use. Like other hypnotics, eszopiclone is a schedule IV drug.
Med Lett Drugs Ther. 2005 Feb 28;47(1203):17-9 |  Show IntroductionHide Introduction

Which Statin?

   
The Medical Letter on Drugs and Therapeutics • Apr 21, 2008  (Issue 1284)
was detectable as early as the first 30 days of the 2-year study. 2 In the simvastatin trial (Phase Z ...
Advertisements for atorvastatin (Lipitor), the market leader facing generic competition, have been in the news recently in the US. Lovastatin, pravastatin and simvastatin are all available generically at a much lower retail price or lower co-pay than atorvastatin.
Med Lett Drugs Ther. 2008 Apr 21;50(1284):29-31 |  Show IntroductionHide Introduction

Drugs for Asthma

   
The Medical Letter on Drugs and Therapeutics • Nov 25, 2024  (Issue 1716)
= hydrofluoroalkane; inh = inhalation; MDI = metered-dose inhaler 1. Approximate WAC for 30 days’ treatment ...
The goal of asthma treatment is to control symptoms, prevent exacerbations, and maintain normal lung function. Management of acute exacerbations in the emergency department is not discussed here.
Med Lett Drugs Ther. 2024 Nov 25;66(1716):185-92   doi:10.58347/tml.2024.1716a |  Show IntroductionHide Introduction

In Brief: Icatibant (Firazyr) for Hereditary Angioedema

   
The Medical Letter on Drugs and Therapeutics • Nov 28, 2011  (Issue 1378)
lasting 2-5 days, typically involving the extremities, gastrointestinal tract, genitalia, face ...
The FDA has approved icatibant (Firazyr – Shire), a selective bradykinin B2 receptor antagonist, for treatment of acute attacks of hereditary angioedema (HAE). HAE is a rare autosomal dominant disorder (estimated prevalence 1:10,000-50,000) in which patients experience recurrent and frequently unpredictable attacks of angioedema lasting 2-5 days, typically involving the extremities, gastrointestinal tract, genitalia, face, oropharynx or larynx. Laryngeal edema may be life-threatening. HAE is usually caused by a mutation of the C1-inhibitor (C1-INH) gene. C1-INH is a serine proteinase...
Med Lett Drugs Ther. 2011 Nov 28;53(1378):96 |  Show IntroductionHide Introduction

In Brief: Calcium and Vitamin D to Prevent Osteoporotic Fractures

   
The Medical Letter on Drugs and Therapeutics • Jun 25, 2012  (Issue 1393)
that there is no evidence that patients with an adequate intake of calcium (1000-1200 mg/day) and vitamin D (600-800 IU ...
The US Preventive Services Task Force (USPSTF) has issued a Draft Recommendation Statement saying, in effect, that community-dwelling women and men should not take calcium and vitamin D supplements for primary prevention of osteoporotic fractures because the evidence that they are helpful is insufficient and they increase the risk of kidney stones. The Medical Letter has said previously that there is no evidence that patients with an adequate intake of calcium (1000-1200 mg/day) and vitamin D (600-800 IU/day) will benefit from taking supplements.11. Drugs for postmenopausal osteoporosis. Treat...
Med Lett Drugs Ther. 2012 Jun 25;54(1393):52 |  Show IntroductionHide Introduction

In Brief: Phentermine (Lomaira) for Weight Loss

   
The Medical Letter on Drugs and Therapeutics • Dec 05, 2016  (Issue 1509)
caps7 15/92 mg Qsymia6 (Vivus) once/d8 ER = extended-release 1. Approximate WAC for 30 days ...
The FDA has approved Lomaira (KVK Tech), an 8-mg tablet formulation of phentermine that can be taken up to three times daily before meals, as an adjunct to lifestyle modifications for weight loss. It is only approved for short-term use (a few weeks) in adults with a body mass index (BMI) ≥30 kg/m2, or with a BMI ≥27 kg/m2 in addition to a weight-related comorbidity such as hypertension, dyslipidemia, or diabetes. Phentermine has been available alone and in combination with topiramate for years.1Lomaira was approved by the FDA under an abbreviated new drug application (ANDA) and is...
Med Lett Drugs Ther. 2016 Dec 5;58(1509):158 |  Show IntroductionHide Introduction

In Brief: Pancreatitis with Eluxadoline (Viberzi) in Patients without a Gallbladder

   
The Medical Letter on Drugs and Therapeutics • Apr 24, 2017  (Issue 1519)
of eluxadoline recommended for such patients (75 mg once/day). Patients considered at risk for pancreatitis ...
The FDA has warned that eluxadoline (Viberzi – Allergan), a mu-opioid receptor agonist and delta-opioid receptor antagonist approved in 2015 for treatment of irritable bowel syndrome with diarrhea (IBS-D),1 should not be used in patients without a gallbladder because of an increased risk of serious pancreatitis.2As of February 2017, the FDA had received reports of 118 cases of serious, nonfatal pancreatitis and 2 deaths associated with use of eluxadoline. Both deaths occurred in patients without a gallbladder who developed severe abdominal pain and vomiting shortly after taking the first...
Med Lett Drugs Ther. 2017 Apr 24;59(1519):70 |  Show IntroductionHide Introduction

Foscarnet

   
The Medical Letter on Drugs and Therapeutics • Jan 10, 1992  (Issue 861)
to achieve an in vivo antiviral effect. CMV RETINITIS — In uncontrolled studies, 14 to 21 days of IV ...
Phosphonoformic acid or foscarnet (Foscavir - Astra), a synthetic antiviral drug, has now been approved by the US Food and Drug Administration for intravenous (IV) treatment of cytomegalovirus (CMV) retinitis in patients with AIDS. CMV retinitis occurs in up to 30% of patients with AIDS and often causes blindness (MD de Smet and RB Nussenbatt, JAMA, 266:3019, Dec 4, 1991).
Med Lett Drugs Ther. 1992 Jan 10;34(861):3-4 |  Show IntroductionHide Introduction

Enoxacin - A New Fluoroquinolone

   
The Medical Letter on Drugs and Therapeutics • Nov 13, 1992  (Issue 883)
, Drugs, 36:32, 1988). One double-blind 14-day trial in 179 men and women with complicated recurrent ...
Enoxacin (en ox' a sin; Penetrex - Rh ne-Poulenc Rorer), a fluoroquinolone antimicrobial for oral use, has now been marketed in the USA for treatment of urinary tract infections and uncomplicated urethral or cervical gonorrhea.
Med Lett Drugs Ther. 1992 Nov 13;34(883):103-5 |  Show IntroductionHide Introduction